I am happy to read that others are finding out about this protocol and it's able to help others.

Unfortunately, my father stopped the protocol only after a month of being on it because the relief of symptoms did not last long enough and he would develop symptoms that were incredibly intolerable for him, he described it as feeling highly irritable and constantly needed help turning and rocking from side to side for temporary relief. At its worst, he was unable to grab his next medication that was even an arm lengths away, he was 90% physically immobile.

We had to discontinue the protocol because it required constant supervion, something my family and I were unable to provide at that time.

I am still hopeful and optimistic about this protocol, but it's lack of data, tests and cost have my family against the fence with it. I am hoping more PDers can chime in with their own success stories.